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Biology Bulletin

, Volume 42, Issue 3, pp 232–238 | Cite as

Specific features of linear growth influencing morphometric parameters of the shell in Margaritifera margaritifera (Bivalvia: Margaritiferidae)

  • A. A. ZotinEmail author
Animal and Human Physiology

Abstract

Interdependence of parameters of shell growth in length and height during ontogeny has been studied in the freshwater pearl mussel M. margaritifera. It has been shown that the results of determining the height-to-length ratio depend on at least two factors: shell corrosion in the apical (umbo) zone and regular, rhythmic deviation of this ratio from values expected from linear regression equation. The first factor may be taken into account by applying an individual correction for each specimen, thereby making the ratio of linear dimensions independent of mussel age and size. The calculation error caused by biological rhythms may be reduced by measuring the greatest possible number of annual rings (≥18). Factors accounting for alternation between periods of prevalent shell growth in length or in height are discussed.

Keywords

Biology Bulletin Annual Ring Shell Growth Shell Height Singular Spectrum Analysis 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Alimov, A.F., Funktsional’naya ekologiya presnovodnykh dvustvorchatykh mollyuskov (Functional Ecology of Freshwater Bivalves), Leningrad: Nauka, 1981.Google Scholar
  2. Bauer, G., Die bionomische strategie der flußperlmuschel, Biol. Unzerer Zeit, 1989, vol. 19, pp. 69–75.CrossRefGoogle Scholar
  3. Bogatov, V.V., Prozorova, L.A., and Starobogatov, Y.I., The family Margaritiferidae (Mollusca; Bivalvia) in Russia, Ruthenica, 2003, vol. 13, no. 1, pp. 41–52.Google Scholar
  4. Bolotov, I.N., Makhrov, A.A., Bespalaya, Yu.V., et al., Results of testing the comparatory method: the curvature of the shell valve frontal section is inappropriate as a systematic character for the freshwater pearl mussel of the genus Margaritifera, Biol. Bull. (Moscow), 2013, vol. 40, no. 2, pp. 221–232.CrossRefGoogle Scholar
  5. Geist, J., Söberberg, H., Karlberg, A., et al., Drainage-independent genetic structure and high genetic diversity of endangered freshwater pearl mussels (Margaritifera margaritifera) in northern Europe, Conserv. Genet., 2010, vol. 11, pp. 1339–1350.CrossRefGoogle Scholar
  6. Helama, S. and Valovirta, I., Ontogenetic morphometrics of individual freshwater pearl mussels (Margaritifera margaritifera (L.)) reconstructed from geometric conchology and trigonometric sclerochronology, Hydrobiologia, 2008, vol. 610, pp. 43–53.CrossRefGoogle Scholar
  7. Ivanter, E.V. and Korosov, A.V., Elementarnaya biometriya: uchebnoe posobie (Elementary Biometrics: A Tutorial), Petrozavodsk: Petrozavodsk. Gos. Univ., 2010.Google Scholar
  8. Kleimenov, S.Yu. and Zotin, A.A., Rhythms of growth and energy metabolism in post-larval ontogeny of Lymnaea stagnalis (Gastropoda, Lymnaeidae), in Mater. nauch. konf., posvyashchennoi 70-letiyu Belomorskoi biol. stantsii MGU: Sb. statei. (Proc. Sci. Conf. Dedicated to the 70th Anniversary of the White Sea Biological Station, Moscow State University), Moscow: Grief i K, 2008, pp. 164–165.Google Scholar
  9. Klishko, O.K., Pearl mussels of the genus Dahurinaia (Bivalvia, Margaritiferidae): Differently sized groups of Margaritifera dahurica Middendorff, 1850, Biol. Bull. (Moscow), 2014, vol. 41, no. 5, pp. 434–443.CrossRefGoogle Scholar
  10. Mina, M.V. and Klevezal, G.A., Rost zhivotnykh (Animal Growth), Moscow: Nauka, 1976.Google Scholar
  11. Naumov, A.D., Dvustvorchatye mollyuski Belogo morya. Opyt ekologo-faunisticheskogo analiza (Bivalves of the White Sea. Experience in Ecofaunistic Analysis), St. Petersburg: Zool. Inst. Ross. Akad. Nauk, 2006.Google Scholar
  12. Naumov, A.D. and Fedyakov, V.V., Application of regression analysis in the taxonomy of bivalves, Tr. Biol. Nauchno-Issled. Inst., 1985, no. 37, pp. 99–110.Google Scholar
  13. Needham, A.E., The Growth Process in Animals, London: Pitman, 1964.Google Scholar
  14. Sergeeva, I.S., Bolotov, I.N., Bespalaya, I.V., et al., Freshwater pearl mussels of the genus Margaritifera (Mollusca: Bivalvia) described as M. elongate (Lamarck, 1819) and M. borealis (Westerlund, 1871) should be classified with M. margaritifera (Linnaeus, 1758), Biol. Bull. (Moscow), 2008, vol 35, no. 1, pp. 102–107.CrossRefGoogle Scholar
  15. Sipachev, S.G., Ritmichnost’ rosta zhivotnykh (Rhythmicity of Animal Growth), Tyumen: Tyumen. Gos. Ped. Inst., 1970.Google Scholar
  16. Zotin, A.I., Termodinamicheskaya osnova reaktsii organizmov na vneshnie i vnutrennie faktory (Thermodynamic Basis of the Response of Organisms to External and Internal Factors), Moscow: Nauka, 1988.Google Scholar
  17. Zotin, A.A., Statistical estimation of allometric coefficients, Biol. Bull. (Moscow), 2000, vol. 27, no. 5, pp. 431–437.Google Scholar
  18. Zotin, A.A., Patterns of growth and energy metabolism in the ontogeny of mollusks, Extended Abstract of Doctoral (Biol.) Dissertation, Moscow: Inst. Dev. Biol. Ross. Akad. Sci., 2009.Google Scholar
  19. Zotin, A.A., The necessity of taking into account the degree of shell corrosion in morphometric studies of bivalves, in Dreissenidy: evolyutsiya, sistematika, ekologiya: Lektsii i materialy dokl. II Mezhdunar. shk.-konf. (Dreissenidae: Evolution, Systematics, and Ecology. Lectures and Proceedings of II Int. School-Conference), Yaroslavl: Kantsler, 2013, pp. 60–62.Google Scholar
  20. Zotin, A.A., Assessment of environmental sustainability by individual growth biorhythms, in Bioraznoobrazie I ustoichivost’ zhivykh sistem: Mater. XIII Mezhdunar. nauch.-prakt. ekol. konf. (Biodiversity and Sustainability of Living Systems: Proc. XIII Int. Sci.-Pract. Ecol. Conf.), Belgorod: ID Belgorod, 2014a, pp. 164–165.Google Scholar
  21. Zotin, A.A., Why linear thermodynamics does describe change of entropy production in living systems?, Nat. Sci., 2014b, vol. 6, pp. 495–502.Google Scholar
  22. Zotin, A.A. and Kirik, E.F., Endogenous rhythms of the energy metabolism rate in two species of freshwater gastropods (Gastropoda, Pulmonata) as a possible mechanism of ontogenetic adaptation, in Tez. dokl. nauch.-prakt. konf. “Adaptatsionnye strategii zhivykh sistem” (Abstr. Sci.-Pract. Conf. “Adaptation Strategies of Living Systems”), Kiev: V.S. Martynyuk, 2012, pp. 43–44.Google Scholar
  23. Zotin, A.A. and Kleimenov, S.Yu., Endogenous rhythms of the specific growth rate of Lymnaea stagnalis (Gastropoda, Lymnaeidae) as a possible mechanism of ontogenetic adaptation of aquatic organisms, in Mater. Vseros. konf. s mezhdunarodnym uchastiem “Fiziologicheskie, biokhimicheskie i molekulyarno-geneticheskie mekhanizmy adaptatsii gidrobiontov” (Proc. Conf. with International Participation “Physiological, Biochemical, and Molecular Genetic Mechanisms of Adaptation of Aquatic Organisms”), Borok: Borok, 2012, pp. 154–156.Google Scholar
  24. Zotin, A.A. and Kleimenov, S.Yu., Endogenous biorhythms of the specific growth rate in individual development of Lymnaea stagnalis (Lymnaeidae, Gastropoda), Biol. Bull. (Moscow), 2013, vol. 40, no. 1, pp. 1–10.CrossRefGoogle Scholar
  25. Zyuganov, V.V. and Zotin, A.A., Pearl mussel Margaritifera margaritifera (Linnaeus, 1758), in Krasnaya Kniga Rossiiskoi Federatsii (zhivotnye) (Red Data Book of the Russian Federation: Animals), Balashikha: Astrel’, 2001, pp. 61–62.Google Scholar
  26. Zyuganov, V.V., Zotin, A.A., and Tret’yakov, V.A., Zhemchuzhnitsy i ikh svyaz’ s lososevymi rybami (Pearl Mussels and Their Relationships with Salmonids), Moscow: TsNIITEIlegprom, 1993.Google Scholar

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© Pleiades Publishing, Inc. 2015

Authors and Affiliations

  1. 1.Kol’tsov Institute of Developmental BiologyRussian Academy of SciencesMoscowRussia

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